Parkinson Disease 5, Autosomal Dominant, Susceptibility To; Park5
Genes related to Parkinson Disease 5, Autosomal Dominant, Susceptibility To; Park5
- UCHL1
Clinical Features
Phenotypes and symptoms related to Parkinson Disease 5, Autosomal Dominant, Susceptibility To; Park5
- Tremor
- Rigidity
- Postural instability
- Bradykinesia
- Resting tremor
Incidence and onset information
— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)— No data available about the known clinical features onset.
Researches and researchers
Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.Parkinson Disease 5, Autosomal Dominant, Susceptibility To; Park5 Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
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Hereditary Spastic Paraplegia Panel.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).
RTN2, SACS, SLC16A2, SLC2A1, KDM5C, SPG11, ATL1, SPAST, SPG7, TFG, ACOX1, TREX1, UCHL1, VAMP1, ERLIN2, CAPN1, BSCL2, SAMHD1, PNPLA6, ERLIN1 , (...)
View the complete list with 59 more genes
Specificity
2 %
Genes
100 % |
Ataxia Exome Panel.
By Genetic Services Laboratory University of Chicago (United States).
BCS1L, RTN2, SACS, SCN1A, SCN2A, SCN8A, SCO1, SDHA, SDHD, SLC16A2, SLC17A5, SLC19A2, SLC1A3, SLC20A2, SLC2A1, SLC6A1, SLC9A1, SLC9A6, SNAP25, SOD1 , (...)
View the complete list with 457 more genes
Specificity
1 %
Genes
100 % |
Parkinson disease 5 (PARK5, sequence analysis of UCHL1 gene).
By CGC Genetics (Portugal).
UCHL1
Specificity
100 %
Genes
100 % |
Parkinson disease (NGS panel for 33 genes).
By CGC Genetics (Portugal).
SLC6A3, SNCA, SNCAIP, SNCB, SYNJ1, TAF1, TH, GIGYF2, UCHL1, VPS35, FBXO7, HTRA2, PINK1, DNAJC6, PARK7, ATP6AP2, LRRK2, CSF1R, ADH1C, DCTN1 , (...)
View the complete list with 12 more genes
Specificity
4 %
Genes
100 % |
Complex Hereditary Spastic Paraplegia Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
SACS, SLC16A2, KDM5C, SPG11, ATL1, SPAST, SPG7, TFG, UCHL1, USP8, VCP, ERLIN2, CAPN1, BSCL2, CCT5, PNPLA6, NIPA1, RAB3GAP2, BICD2, GJC2 , (...)
View the complete list with 50 more genes
Specificity
2 %
Genes
100 % |
Hereditary Spastic Paraplegia Comprehensive Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
RTN2, SACS, SLC16A2, KDM5C, SPG11, ATL1, SPAST, SPG7, TFG, UCHL1, USP8, VCP, ERLIN2, CAPN1, BSCL2, CCT5, PNPLA6, ERLIN1, NIPA1, RAB3GAP2 , (...)
View the complete list with 60 more genes
Specificity
2 %
Genes
100 % |
Parkinson Disease Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
SLC6A3, SNCA, SPR, SYNJ1, TAF1, GIGYF2, UCHL1, VPS35, FBXO7, HTRA2, PINK1, DNAJC6, PARK7, RAB39B, LRRK2, CHCHD2, VPS13C, ATP13A2, EIF4G1, GBA , (...)
View the complete list with 4 more genes
Specificity
5 %
Genes
100 % |
Parkinson Disease and Parkinsonism Sequencing Panel with CNV Detection.
By PreventionGenetics PreventionGenetics (United States).
SLC20A2, SLC6A3, SNCA, SNCB, SPG11, SPR, SYNJ1, TAF1, TARDBP, TWNK, TH, GIGYF2, UCHL1, XPR1, VPS35, FBXO7, HTRA2, PINK1, DNAJC6, CHCHD10 , (...)
View the complete list with 48 more genes
Specificity
2 %
Genes
100 % |
You can get up to 11 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
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